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Oral Anticoagulation in Patients With Atrial High-Rate Episodes: Focus on Clinical Implications.
Dimou, Smaro; Mystakidi, Vasiliki C; Chiotis, Sotirios; Daios, Stylianos; Kalantzis, Charalambos; Milaras, Nikias; Karamitsos, Theodoros D; Karvounis, Haralambos; Efthimiadis, Georgios; Paraskevaidis, Stylianos.
Afiliação
  • Dimou S; First Department of Cardiology, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
  • Mystakidi VC; Department of Cardiology, 424 General Military Hospital, Thessaloniki, GRC.
  • Chiotis S; Third University Department of Cardiology, National and Kapodistrian University of Athens, Athens, GRC.
  • Daios S; Department of Cardiology, 424 General Military Hospital, Thessaloniki, GRC.
  • Kalantzis C; First Department of Cardiology, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
  • Milaras N; First University Department of Cardiology, National and Kapodistrian University of Athens, Athens, GRC.
  • Karamitsos TD; First University Department of Cardiology, National and Kapodistrian University of Athens, Athens, GRC.
  • Karvounis H; First Department of Cardiology, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
  • Efthimiadis G; First Department of Cardiology, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
  • Paraskevaidis S; First Department of Cardiology, AHEPA Hospital, Aristotle University of Thessaloniki, Thessaloniki, GRC.
Cureus ; 15(10): e46686, 2023 Oct.
Article em En | MEDLINE | ID: mdl-37942367
ABSTRACT
Background Although previous studies showed that atrial high-rate episodes (AHREs) are associated with a higher risk of developing incident atrial fibrillation (AF) and thromboembolic events, their clinical significance is still unclear. The purpose of this study was to define whether there is any clinical impact on the occurrence of ischemic and hemorrhagic events in patients with AHREs and initiation of oral anticoagulation (OAC). Methodology Patients with AHREs who had received cardiac implantable electronic devices (CIEDs, i.e., dual-chamber pacemaker [PM] or implantable cardioverter defibrillator [ICD]) were included in the study. OAC initiation was decided by the assistant doctor. Patients who received OACs comprised the OAC group, while patients who were not referred for OAC initiation were included in the control group. The primary endpoint was the time to the event of the occurrence of thromboembolic events (thromboembolic event-free survival). Results A total of 154 individuals (77 in each group) were enrolled in the study, with a mean age of 72.5 years. The mean follow-up period for the OAC group was 19.1 months and for the control group, 18.9 months (P = 0.9). Thromboembolic events were noticed only in seven patients. Six of them were in the control group, and only one in the OAC group (P = 0.05). Major bleeding events were noticed in five patients, one of whom was in the control group and the rest in the OAC group (P = 0.17). Conclusions OAC therapy in patients with AHREs was not associated with a significant difference in the risk of thromboembolic and bleeding events. Baseline patient characteristics and AHRE duration may be useful to intensify the monitoring and management of patients with AHREs. Bleeding events may be indicators of cancer in patients with AHREs receiving OACs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2023 Tipo de documento: Article